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A Study to Assess the Pharmacokinetics, Safety, and Efficacy of Two Doses of Bimekizumab in Adolescent Study Participants With Moderate to Severe Plaque Psoriasis
Sponsor: UCB Biopharma SRL
Summary
The purpose of the study is to assess th pharmacokinetics (PK) of bimekizumab administered subcutaneously (sc) in adolescents with moderate to severe plaque psoriasis (PSO).
Official title: A Multicenter, Open-Label, Randomized Study to Assess the Pharmacokinetics, Safety, and Efficacy of Two Doses of Bimekizumab in Adolescent Study Participants With Moderate to Severe Plaque Psoriasis
Key Details
Gender
All
Age Range
12 Years - 17 Years
Study Type
INTERVENTIONAL
Enrollment
41
Start Date
2021-04-06
Completion Date
2025-03-12
Last Updated
2026-05-18
Healthy Volunteers
No
Conditions
Interventions
bimekizumab
Study participants will receive subcutaneously administered bimekizumab (BKZ) at pre-specified time points during the study.
Locations (11)
Ps0020 50344
Indianapolis, Indiana, United States
Ps0020 50359
Cypress, Texas, United States
Ps0020 50354
Calgary, Canada
Ps0020 50357
St. John's, Canada
Ps0020 40645
Frankfurt, Germany
Ps0020 40626
Bialystok, Poland
Ps0020 40625
Lodz, Poland
Ps0020 40396
Rzeszów, Poland
Ps0020 40335
Warsaw, Poland
Ps0020 40333
Wroclaw, Poland
Ps0020 40334
Wroclaw, Poland